1. Dancis J, Hutzler J, Cox RP et al (1976) Multiple enzyme defects in familial hyperlysinemia. Pediatr Res 10:686–691
2. Cox RP (2001) Errors of lysine metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill Inc, New York, pp 1965–1970
3. Cox RP, Dancis J (1995) Errors of lysine metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill Inc, New York, pp 1233–1238
4. Cox RP, Markovitz PJ, Chuang DT (1986) Familial hyperlysinemias-multiple enzyme deficiencies associated with the bifunctional aminoadipic semialdehyde synthase. Trans Am Clin Climatol Assoc 97:69–81
5. Hoffmann GF (2006) Cerebral organic acid disorders and other disorders of lysine catabolism. In: Fernandes J, Saudubray J-M, van den Berghe G, Walter JH (eds) Inborn metabolic diseases. Springer, Heidelberg, pp 293–306